Production of Dictyostelium discoideum Hybrid Type Enzyme SteelyA in the Diatom Phaeodactylum tricornutum

The bioproduction of high-value molecules offers a sustainable and cost-effective alternative to traditional extraction and chemical synthesis, particularly for complex metabolites like cannabinoids (CBs), which have therapeutic potential for neurodegenerative diseases. The marine diatom Phaeodactylum tricornutum presents a promising chassis for CB biosynthesis due to its high lipid content, essential building blocks to biosynthesize CBs. In this study, we explored the feasibility of producing olivetolic acid (OA), the key CB precursor, using a hybrid-type polyketide synthase, SteelyA, from Dictyostelium discoideum. Unlike the native Cannabis sativa enzymes—tetraketide synthase and olivetolic acid cyclase—which exhibit low productivity and stability in diatoms, SteelyA was expected to offer an alternative biosynthetic route. Heterologous production in P. tricornutum resulted in a C-terminal fragment of the SteelyA enzyme, suggesting partial expression or processing of the very high-molecular-weight (352 kDa) SteelyA protein over six months without affecting cellular growth. However, HPLC-MS analysis did not detect intracellular OA or its derivatives in vivo and in vitro, suggesting enzymatic inactivity or metabolic limitations. These negative findings highlight the need for further investigation into the metabolic and proteomic requirements for CB precursor biosynthesis in diatoms, guiding future optimization strategies for sustainable cannabinoid production.

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Publication Details

Journal
Applied Sciences
Published
2025-10-31
DOI
https://doi.org/10.3390/app152111679
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39

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article

Production of Dictyostelium discoideum Hybrid Type Enzyme SteelyA in the Diatom Phaeodactylum tricornutum

Isabel Desgagné‐Penix, Basanta Lamichhane, Fatma Meddeb‐Mouelhi, Sarah‐Eve Gélinas et al.
1 citations
Applied Sciences
Microbial Natural Products and Biosynthesis
1.39
article

Production of Dictyostelium discoideum Hybrid Type Enzyme SteelyA in the Diatom Phaeodactylum tricornutum

Isabel Desgagné‐Penix, Basanta Lamichhane, Fatma Meddeb‐Mouelhi, Sarah‐Eve Gélinas, Natacha Mérindol, Alexandre Custeau, Nicolas Sene
article en
1 citations

Abstract

The bioproduction of high-value molecules offers a sustainable and cost-effective alternative to traditional extraction and chemical synthesis, particularly for complex metabolites like cannabinoids (CBs), which have therapeutic potential for neurodegenerative diseases. The marine diatom Phaeodactylum tricornutum presents a promising chassis for CB biosynthesis due to its high lipid content, essential building blocks to biosynthesize CBs. In this study, we explored the feasibility of producing olivetolic acid (OA), the key CB precursor, using a hybrid-type polyketide synthase, SteelyA, from Dictyostelium discoideum. Unlike the native Cannabis sativa enzymes—tetraketide synthase and olivetolic acid cyclase—which exhibit low productivity and stability in diatoms, SteelyA was expected to offer an alternative biosynthetic route. Heterologous production in P. tricornutum resulted in a C-terminal fragment of the SteelyA enzyme, suggesting partial expression or processing of the very high-molecular-weight (352 kDa) SteelyA protein over six months without affecting cellular growth. However, HPLC-MS analysis did not detect intracellular OA or its derivatives in vivo and in vitro, suggesting enzymatic inactivity or metabolic limitations. These negative findings highlight the need for further investigation into the metabolic and proteomic requirements for CB precursor biosynthesis in diatoms, guiding future optimization strategies for sustainable cannabinoid production.

Applied SciencesVol. 15(21)
Université du Québec à Trois-Rivières (CA)
Université du Québec à Trois-Rivières, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 15%
Microbial Natural Products and Biosynthesis
1.39
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